German drug major Bayer (BAY: DE) yesterday announced the eagerly-awaited results from the pivotal, double-blind Phase III, ROCKET AF trial, which demonstrated that its Xarelto (rivaroxaban), under development with the USA’s Johnson & Johnson (NYSE: JNJ) was superior to warfarin in reducing the risk of stroke and non-central nervous system systemic embolism in patients with atrial fibrillation (AF).
Importantly, rates of bleeding were similar to warfarin, and bleeding events most concerning to physicians and patients, including intracranial hemorrhage, critical organ bleed, and bleeding-related death, were significantly lower in the rivaroxaban group. The results were presented at the American Heart Association Scientific Sessions 2010 in Chicago, and the news saw Bayer’s shares jump as much as 6.4% to 56.58 euros in afternoon trading yesterday, though closing just 3.9% higher at 56.13 euros.
“Conservative” sales potential of $2.7 billion
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze